R&D

GMP Center

Trust in cell therapy begins in the production environment.

Equipped with state-of-the-art facilities, we simultaneously conduct advanced biopharmaceutical production and clinical research, in a strictly controlled environment, taking responsibility for the safety of every single cell. taking responsibility for the quality of every single cell. Cell therapeutics at 4,000 lots per year, annual production capacity and operates a stable 19,000-vial storage system, enabling rapid and consistent supply. with production facilities for stem cells and immune cells operated fully separated and independent, blocking cross-contamination at the source and keeping each maintaining environments optimized for each cell type. From manufacturing to storage and supply, completed within one trusted system—that is the core strength of our GMP facility. that is our core competitive strength.

①

Clean Room

Aseptic Workroom

A highly controlled, clean production space that completely blocks external contaminants. Temperature, humidity, and differential pressure are precisely controlled, and the entire cell production process takes place within this environment. Facility design that meets GMP standards guarantees consistent quality.

②

Cell Culture Room

All cell culture processes are performed inside biosafety cabinets (BSC), thoroughly blocking external and cross-contamination. CO2 incubators precisely maintain in-body conditions—optimal temperature, CO2 concentration, and humidity—to maximize cell survival and activity. The entire process of stem cell and immune cell culture takes place in this room.

③

Cell Analysis Room

Product quality is evaluated with a range of analytical instruments under cell therapeutic quality test standards. This is the core quality-control space that verifies key quality attributes—characteristics, purity, sterility, and safety—to supply reliable cell therapeutics.

④

PCR / Molecular Diagnostics Room

PCR Room

A space that verifies cell purity, identity, and sterility with molecular-level precision. Real-time quantitative PCR (Real-Time PCR) equipment analyzes gene expression and judges quality conformity before final release. All analyses are performed rigorously under standardized procedures.

⑤

Cryogenic (Liquid Nitrogen) Storage Room

Cryogenic Storage Room

A space where cells are stored stably for the long term at ultra-low temperatures of -196 degrees C. It preserves cell activity and function without damage and enables immediate supply when needed, supporting storage capacity of up to 19,000 vials.

Cryogenic (Liquid Nitrogen) Storage Room

⑥

Air Handling Unit (AHU) Room

Air Handling Unit Room

Core environmental-control equipment that integrally manages the temperature, humidity, cleanliness, and pressure of air within the GMP facility. It precisely purifies and conditions outside air to supply a uniform clean environment across all production zones. Positive and negative pressure management blocks contamination transfer between zones at the source.